subject area of
- A Rapid Polymerase Chain Reaction-Based Screening Method for Identification of All Expanded Alleles of the Fragile X (FMR1) Gene in Newborn and High-Risk Populations Academic Article
- A family with two female siblings with compound heterozygousFMR1premutation alleles Academic Article
- A genome-wide Drosophila epithelial tumorigenesis screen identifies Tetraspanin 29Fb as an evolutionarily conserved suppressor of Ras-driven cancer Academic Article
- A high-throughput protocol for mutation scanning of the BRCA1 and BRCA2 genes Academic Article
- A kinome RNAi screen in Drosophila identifies novel genes interacting with Lgl, aPKC, and CrB cell polarity genes in epithelial tissues Academic Article
- A review of fragile X premutation disorders: Expanding the psychiatric perspective Academic Article
- A simple tool for identifying unaffected women at a moderately increased or potentially high risk of breast cancer based on their family history Academic Article
- Changes in Physical Activity Following a Genetic-Based Internet-Delivered Personalized Intervention: Randomized Controlled Trial (Food4Me) Academic Article
- Detection of NPM1 exon 12 mutations and FLT3 – internal tandem duplications by high resolution melting analysis in normal karyotype acute myeloid leukemia Academic Article
- FMR1 alleles in Tasmania: a screening study of the special educational needs population Academic Article
- FMR1 gray-zone alleles: Association with Parkinson's disease in women? Academic Article
- Fragile X-associated tremor/ataxia syndrome: Clinical features, genetics, and testing guidelines Academic Article
- Fragile X–related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study Academic Article
- G1738R is a BRCA1 founder mutation in Greek breast/ovarian cancer patients: evaluation of its pathogenicity and inferences on its genealogical history Academic Article
- Genetic cluster of fragile X syndrome in a Colombian district Academic Article
- Genotype-phenotype assessment in autosomal recessive arrhythmogenic right ventricular cardiomyopathy (Naxos disease) caused by a deletion in plakoglobin Academic Article
- High resolution melting analysis for rapid and sensitive EGFR and KRAS mutation detection in formalin fixed paraffin embedded biopsies Academic Article
- High-Risk Fragile X Screening in Guatemala: Use of a New Blood Spot Polymerase Chain Reaction Technique Academic Article
- Identification of Expanded Alleles of the FMR1 Gene Among High-Risk Population in Indonesia by Using Blood Spot Screening Academic Article
- Identification of expanded alleles of the FMR1 gene in the CHildhood Autism Risks from Genes and Environment (CHARGE) study Academic Article
- Incorporation of somatic BRAF mutation testing into an algorithm for the investigation of hereditary non-polyposis colorectal cancer Academic Article
- Methylation Analysis in Newborn Screening for Fragile X Syndrome—Reply Letter
- Methylation-sensitive, single-strand conformation analysis (MS-SSCA): A rapid method to screen for and analyze methylation Academic Article
- Molecular screening of sheep for bovine spongiform encephalopathy Academic Article
- Mutational analysis of BMP15 and GDF9 as candidate genes for premature ovarian failure Academic Article
- Mutational analysis of betaglycan/TGF-βRIII in premature ovarian failure Academic Article
- Newborn Screening for Fragile X Syndrome Academic Article
- Newborn screening and cascade testing forFMR1mutations Academic Article
- Novel DNA sequence variants in the hHR21 DNA repair gene in radiosensitive cancer patients Academic Article
- Offering pregnant women different levels of genetic information from prenatal chromosome microarray: a prospective study Academic Article
- Pharmacogenetic screening of Indigenous Australians Academic Article
- Prognostic serum miRNA biomarkers associated with Alzheimer's disease shows concordance with neuropsychological and neuroimaging assessment Academic Article
- Proton pump inhibitors, genetic polymorphisms and response to clopidogrel therapy Academic Article
- Psychiatric Phenotype of the Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS) in Males Academic Article
- Public health, private genes: The social context of genetic biotechnologies Academic Article
- Screen for Excess FMR1 Premutation Alleles Among Males With Parkinsonism Academic Article
- Screen for expandedFMR1 alleles in patients with essential tremor Academic Article
- Screening Procedure for Pichia pastoris Clones Containing Multiple Copy Gene Inserts Academic Article
- Screening for Expanded Alleles of the FMR1 Gene in Blood Spots from Newborn Males in a Spanish Population Academic Article
- Screening for the Presence of FMR1 Premutation Alleles in Women With Parkinsonism Academic Article
- Sleep apnea in fragile X premutation carriers with and without FXTAS Academic Article
- The cost-benefit of genomic testing of heifers and using sexed semen in pasture-based dairy herds Academic Article
- The prediction of disease risk in genomic medicine Academic Article
- Using imputed whole-genome sequence data to improve the accuracy of genomic prediction for parasite resistance in Australian sheep Academic Article
- Volumetric brain changes in females with fragile X-associated tremor/ataxia syndrome (FXTAS) Academic Article